340618

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Unsymmetrical tetradentate Schiff base complexes derived from 2, 3-diaminophenol and salicylaldehyde or 5-bromosalicylaldehyde.

Ourari A, et al.

Transition Metal Chemistry, 31(2), 169-175 (2006)

Transition Met. Chem. (London), 31, 169-169 (2006)

On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines.

Andreas Schmidt et al.

Organic & biomolecular chemistry, 1(23), 4342-4350 (2003-12-20)

2,3-Diaminophenol 4, 3,4-diaminophenol 5, 4-methoxy-1,2-diaminobenzene 6, 3,4-diaminobenzenethiol 7, 2,3-diaminobenzoic acid 8, and 3,4-diaminobenzoic acid 9 were reacted with 2,4-pentanedione to yield the corresponding benzo[b][1,4]diazepinium salts, respectively. The hydroxy-benzo[b][1,4]diazepinium salts 17 and 18 do not form mesomeric betaines (MB) on deprotonation.

1,5-Benzoxazepines vs 1,5-benzodiazepines. one-pot microwave-assisted synthesis and evaluation for antioxidant activity and lipid peroxidation inhibition.

Constantinos G Neochoritis et al.

Journal of medicinal chemistry, 53(23), 8409-8420 (2010-11-06)

Amino-1,5-benzoxazepines 2 and 5 and hydroxyl-1,5-benzodiazepines 3 and 6 have been synthesized in one-pot solvent-free conditions from 2,3-diaminophenol and ketones through microwave assisted acid catalysis, the benzoxazepine/benzodiazepine ratio depending on the R(1) and R(3) aryl substituents. The otherwise inaccessible and

Pd(II) and Pt(II) complexes with aromatic diamines: study of their interaction with DNA.

M Pérez-Cabré et al.

Journal of inorganic biochemistry, 98(3), 510-521 (2004-02-28)

Pd(II) and Pt(II) new complexes with simple aromatic diamines were synthesised and characterised with the aim of studying their possible antitumour activity. The aromatic diamines chosen were 2,3-diaminotoluene (2,3 dat), 3,4-diaminotoluene (3,4 dat), 4,5-diaminoxylene (4,5 dax) and 2,3-diaminophenol (2,3 dap).

Electropolymerization of 2, 3-diaminophenol.

Del Valle MA, et al.

Journal of Polymer Science Part A: Polymer Chemistry, 38(9), 1698-1703 (2000)

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